Citations Report

Citation Index - Clinical Investigation [920 Articles]

The articles published in Clinical Investigation have been cited 920 times by eminent researchers all around the world. Following is the list of articles that have cited the articles published in Clinical Investigation.

  • Ricotti V, Jägle H, Theodorou M, Moore AT, Muntoni F, Thompson DA.(2016) Ocular and neurodevelopmental features of Duchenne muscular dystrophy: a signature of dystrophin function in the central nervous system. European Journal of Human Geneticsx ;24:562-568.

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  • Goemans NM, Tulinius M, van den Hauwe M, Kroksmark AK, Buyse G.,et.al.. (2016) Long-term efficacy, safety, and pharmacokinetics of drisapersen in Duchenne muscular dystrophy: results from an open-label extension study. PloS one ;11:e0161955.

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  • Li Y, Zhang S, Zhang X, Li J, Ai X, Zhang L, Yu D, Ge S, Peng Y, Chen X. (2014) Blunted cardiac beta-adrenergic response as an early indication of cardiac dysfunction in Duchenne muscular dystrophy. Cardiovascular research ;103:60-71.

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  • Heslop E, Csimma C, Straub V, McCall J, Nagaraju K, Wagner KR, Caizergues D, Korinthenberg R, Flanigan KM, Kaufmann P, McNeil E. (2015)The TREAT-NMD advisory committee for therapeutics (TACT): an innovative de-risking model to foster orphan drug development. Orphanet journal of rare diseases ;10:49.

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  • Geirs DP, Pottegård A, Halldórsson M, Zoëga H (2014 ) A Nationwide Study of Attention‐Deficit/Hyperactivity Disorder Drug Use among Adults in Iceland 2003–2012. Basic & clinical pharmacology & toxicology 115: 417-422.

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  • Geirs DP, Pottegård A, Halldórsson M, Zoëga H (2014) A Nationwide Study of ADHD Drug Use among Adults in Iceland 2003-2012 .

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  • Oonk S, Spitali P, Hiller M, Switzar L, Dalebout H, Calissano M, Lochmüller H, Aartsma‐Rus A, Hoen P, Burgt YE.(2016) Comparative mass spectrometric and immunoassay‐based proteome analysis in serum of Duchenne muscular dystrophy patients. PROTEOMICS-Clinical Applications ;10:290-299.

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  • Ricotti V, Muntoni F, Voit T.(2015) Challenges of clinical trial design for DMD. Neuromuscular Disorders ;25:932-935.

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  • Weimer K, Enck P (2014) Traditional and innovative experimental and clinical trial designs and their advantages and pitfalls. InPlacebo 237-272.

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  • Fischer D, Hafner P, Rubino D, Schmid M, Neuhaus C, Jung H, Bieri O, Haas T, Gloor M, Fischmann A, Bonati U. (2016) The 6-minute walk test,motor function measure and quantitative thigh muscle MRI in Becker muscular dystrophy: A cross-sectional study. Neuromuscular Disorders ;26:414-422.

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  • Rosenberg PB, Drye LT, Porsteinsson AP, Pollock BG, Devanand DP, et al. (2015) Change in agitation in Alzheimer's disease in the placebo arm of a nine-week controlled trial. International psychogeriatrics 27: 2059-2067.

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  • Hafner P, Bonati U, Rubino D, Gocheva V, Zumbrunn T, Gueven N, Fischer D.(2016) Treatment with L-citrulline and metformin in Duchenne muscular dystrophy: study protocol for a single-centre, randomised, placebo-controlled trial. Trials ;17:389.

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  • Iovieno N, Nierenberg AA, Parkin SR, Kim DJ, Walker RS, et al. (2016 ) Relationship between placebo response rate and clinical trial outcome in bipolar depression. Journal of psychiatric research 74: 38-44.

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  • Wei Y, Speechley K, Campbell C.(2015) Health-Related Quality of Life in Children with DuchenneMuscular Dystrophy: A Review. Journal of Neuromuscular Diseases;2:313-324.

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  • Wang JJ, Ivanova A (2014 ) Dose finding with the sequential parallel comparison design. Journal of biopharmaceutical statistics 24: 1091-1101.

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  • Soto M, Abushakra S, Cummings J, Siffert J, Robert P, et al. (2015) Progress in Treatment Development for Neuropsychiatric Symptoms in Alzheimer’s Disease: Focus on Agitation and Aggression. A Report from the EU/US/CTAD Task Force. The journal of prevention of Alzheimer's disease 2:184.

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  • Rosenkranz GK (2016) Remarks on designs enriching for placebo non-responders. Clinical Trials 13: 338-343.

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  • Silverman RK, Ivanova A (2017 ) Sample size re-estimation and other mid-course adjustments with sequential parallel comparison design. Journal of Biopharmaceutical Statistics.

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  • Wilsey B, Deutsch R, Marcotte TD ( 2016 ) Maintenance of Blinding in Clinical Trials and the Implications for Studying Analgesia Using Cannabinoids. Cannabis and Cannabinoid Research 1: 139-148.

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  • Ivanova A, Zhang Z, Thompson L, Yang Y, Kotz RM, et al. (2016 ) Can sequential parallel comparison design and two-way enriched design be useful in medical device clinical trials?. Journal of Biopharmaceutical Statistics 26: 167-177.

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  • Toniolo RA (2016) Ensaio clínico randomizado, duplo-cego, controlado com placebo, de monoidrato de creatina como terapia adjuvante na depressão bipolar (Doctoral dissertation, Universidade de São Paulo).

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  • Malheiros SR, Ribeiro DC, Alvarez MP, de Freitas BL, et.al. (2015)Motor Learning in Duchenne Muscular Dystrophy, a Literature Review. International Archives of Medicine;8.

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  • da Silva TD, de Oliveira EP, Balbino GC, de Souza JM, Capelini CM, Guarnieri R, de Abreu Lc.,et.al. Pegboard task in Duchenne muscular dystrophy. HealthMED.:365.

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  • Bushby K. (2015) Looking forward to new therapies: a personal perspective on the translational landscape for muscular dystrophies. Journal of Neuromuscular Diseases;2:S83. View at Publisher | View at Google Scholar
  • López Villar E, Wu D, Cho WC, Madero L, Wang X (2014) Proteomics‐based discovery of biomarkers for paediatric acute lymphoblastic leukaemia: challenges and opportunities. Journal of cellular and molecular medicine 18: 1239-1246.

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  • Doussau A, Geoerger B, Jiménez I, Paoletti X (2016 ) Innovations for phase I dose-finding designs in pediatric oncology clinical trials. Contemporary clinical trials. 47: 217-227.

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  • Buckon C, Sienko S, Bagley A, Sison-Williamson M, Fowler E, Staudt L, Heberer K, McDonald CM, Sussman M.(2016) Can Quantitative Muscle Strength and Functional Motor Ability Differentiate the Influence of Age and Corticosteroids in Ambulatory Boys with Duchenne Muscular Dystrophy?. PLoS Currents ;8.

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  • Lewis LM, Graffeo C, Crosley P, Klausner HA, Clark CL, et al. (2015 ) Ecallantide for the acute treatment of angiotensin-converting enzyme inhibitor–induced angioedema: a multicenter, randomized, controlled trial. Annals of emergency medicine 65: 204-213.

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  • Mercuri E, Baranello G, Battini R, Berardinelli A, Bertini E.,et.al..(2016) Registries versus tertiary care centers. Neuromuscular Disorders ;26(4-5):261-3.

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  • Craig TJ, Li HH, Riedl M, Bernstein JA, Lumry WR, et al. (2015 ) Characterization of anaphylaxis after ecallantide treatment of hereditary angioedema attacks. The Journal of Allergy and Clinical Immunology: In Practice 3: 206-212.

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  • Fischer D, Hafner P, Rubino D, Schmid M. The 6-minute walk test, motor function measure and quantitative thigh. Imaging ;38:619-624.

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  • Bernstein JA, Moellman JJ, Collins SP, Hart KW, Lindsell CJ ( 2015 ) Effectiveness of ecallantide in treating angiotensin-converting enzyme inhibitor–induced angioedema in the emergency department. Annals of Allergy, Asthma & Immunology 114: 245-249.

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  • Travlos V, Patman S, Wilson A, Simcock G, Downs J.(2016) Quality of life and psychosocial wellbeing in youth with neuromuscular disorders who are wheelchair users: A systematic review. Archives of Physical Medicine and Rehabilitation.

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  • Shklyar I. Electrical Impedance Myography And Quantitative Ultrasound As Biomarkers In Duchenne Muscular Dystrophy.

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  • Pelentsov LJ, Fielder AL, Esterman AJ (2016 ) The supportive care needs of parents with a child with a rare disease: a qualitative descriptive study. Journal of pediatric nursing 31: e207-e218.

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  • Vahedi L, Jabarpoor-Bonyadi M, Ghojazadeh M, Hazrati H, Rafeey M (2016) Association between outcomes and demographic factors in an Azeri Turkish population with cystic fibrosis: a cross-sectional study in Iran from 2001 through . Iranian Red Crescent Medical Journal 18.

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  • Goemans N, Vanden Hauwe M, Signorovitch J, Swallow E, Song J. (2016) Individualized Prediction of Changes in 6-Minute Walk Distance for Patients with Duchenne Muscular Dystrophy. PloS one;11:e0164684.

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  • Dunn AL (2016) Mapping Patient and Caregiver Involvement across the Orphan Drug Lifecycle and in Programs that Provide Access to Promising Therapies While Ensuring Prudent use of Scarce Health Care Resources (Doctoral dissertation, University of Alberta).

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  • Foster CS, Kothari S, Anesi SD, Vitale AT, Chu D, et al. (2016) The Ocular Immunology and Uveitis Foundation preferred practice patterns of uveitis management. Survey of ophthalmology 61: 1-7.

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  • Pigula AJ, Wu JS, Gilbertson MW, Darras BT, Rutkove SB, Anthony BW. (2016) Force-controlled ultrasound to measure passive mechanical properties of muscle in Duchenne muscular dystrophy. InEngineering in Medicine and Biology Society (EMBC), 2016 IEEE 38th Annual International Conference IEEE.. 2865-2868

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  • Olga Ceron MD, FACR CS (2011) Recent Advances in Uveitic Glaucoma. Ophthalmology 26: 4-5.

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  • Koppaka S, Shklyar I, Rutkove SB, Darras BT, Anthony BW, Zaidman CM, Wu JS. (2016) Quantitative Ultrasound Assessment of Duchenne Muscular Dystrophy Using Edge Detection Analysis. Journal of Ultrasound in Medicine;35:188918-97.

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  • Taheri T, Seyed N, Mizbani A, Rafati S ( 2016 ) Leishmania-based expression systems. Applied microbiology and biotechnology 100: 7377-7385.

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  • Seyed N, Taheri T, Rafati S (2016) Post-Genomics and Vaccine Improvement for Leishmania. Frontiers in microbiology 7.

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  • Hogarth MW. α-Actinin-3: a novel genetic modifier of duchenne muscular dystrophy.

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  • Keating GM (2015 ) Aflibercept: A Review of Its Use in Diabetic Macular Oedema. Drugs 75: 1153-1160.

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  • Silverstein CA. A Patient-Report Registry to Study Outcomes in a Rare Genetic Disease: DuchenneConnect.

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  • Rutkove SB, Kapur K, Zaidman C, Wu JS, Pasternak A, Madabusi L, et.al,. Electrical impedance myography for assessment of Duchenne muscular dystrophy. Annals of Neurology.

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  • Goemans N, Tulinius M, Kroksmark AK, Wilson R, van den Hauwe M, Campion G. (2016) Comparison of ambulatory capacity and disease progression of duchenne muscular dystrophy subjects enrolled in the drisapersen DMD114673 study with a matched natural history cohort of subjects on daily corticosteroids. Neuromuscular Disorders.

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  • Teng T, Xu S, Chen Q, Chen F, Li X, et al. (2016) iegesbeckia pubescens ameliorates experimental ulcerative colitis in rats by modulating PPARγ. Int J Clin Exp Med 23082-23091.

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